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Clinical Trials/CTRI/2025/04/083811
CTRI/2025/04/083811RecruitingNot Applicable

Systemic and Tumor Immune Response during pelvic (chemo)Radiation and or brachytherapy for cervical cancer (STIRR Cervix Study)

Tata Memorial Hospital1 site in 1 country110 target enrollmentStarted: April 15, 2025Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
110
Locations
1
Primary Endpoint
Objective 1: To study the multi-time point interaction between radiotherapy for cervical cancer and impact on systemic immune cells.

Study Overview

Brief Summary

Cervical cancer is the second most common cancer in Indian women. This cancer is mostly associated with persistence of human papillomavirus infection and hence the role of immune system is thus relevant. The pelvic bones region which houses a lot of immune cells receives a high dose of radiation as part of their treatment. Therefore we are conducting a study that will assess how immune system is affected by pelvic radiotherapy (various radiotherapy doses and volume) in cervical cancer.

A total of 110 patients will participate in the study from Tata Memorial Centre. We expect to complete the accrual in a period of 30 months from our department. All patients will receive radiation followed by brachytherapy as a standard of care. Concurrent chemotherapy will be given when indicated. Once patients gives consent to participate in the study, they will be allotted into a study group depending on their treatment plan. The study has three main cohorts. Cohort A is Pelvic RT which is further divided into 3 sub-cohorts - Radical (45Gy/25#), Palliative A (25Gy/5#), Palliative B (30Gy/3#). Cohort B is Pelvic + Paraaortic RT (45Gy/25#). Cohort C is Reirradiation cohort which is further divided into 3 sub-cohorts - Proton (40Gy/20#), Photon (25-30Gy/5-6#), SFRT (45Gy/25#). Patient will then go ahead with planned radiation treatment. According to the group in whom the patient is allotted, samples will be taken at baseline and after receiving radiation to study the immune profile.

Variation in immune response will be studied in each cohort. Furthermore, different cohorts will be studied against each other to understand how different doses, field volumes and techniques of radiotherapy impact body’s immunity. Additionally, for each of the recruited cohorts, a three-year disease-free survival will be reported based on the immune cell composition before and after radiation therapy. After completing study related procedure patients will continue follow up as per standard policy at every 3 months up to 24 months and every 6 months for next 24 months post treatment completion. They will be checked clinically at every follow up visit.

The outcome of the study would be useful in improving the quality of radiation treatment and in reducing disease recurrence and improving survival in patients with cervical cancer.

Study Design

Study Type
Observational

Eligibility Criteria

Ages
18.00 Year(s) to 90.00 Year(s) (—)
Sex
Female

Inclusion Criteria

  • Common Inclusion Criteria
  • Age 18 years and above.
  • Ability to tolerate full course of pelvic radiotherapy and or chemotherapy and or brachytherapy
  • Ability to understand and willingness to sign an informed consent document.
  • Should be willing to undergo extra biopsies and blood samples collection for translational research study.
  • Patients diagnosed with LACC Stage IB2 to IIIC1, as per FIGO 2018 Classification for Radical Cohort.
  • Stage IIIB to IVA where palliative RT is indicated for palliative cohort.
  • No previous irradiation to the pelvis or chemo therapy.
  • No previous irradiation to the pelvis or chemotherapy.
  • Patients diagnosed with gynecological cancer and presenting with need of infield radiation.
  • Planned for reirradiation.

Exclusion Criteria

  • Severe medical condition impairing complete treatment delivery.
  • Patients with immunocompromised states or active infection.
  • Patients on immunosuppressive drugs for other medical conditions.

Outcomes

Primary Outcomes

Objective 1: To study the multi-time point interaction between radiotherapy for cervical cancer and impact on systemic immune cells.

Time Frame: Baseline, Week 1, Week 3, Month 3

Objective 2: To study the multi-time point interaction between radiotherapy for cervical cancer and impact on tumor infiltrating immune cells and PD-L1 expression.

Time Frame: Baseline, Week 1, Week 3, Month 3

Secondary Outcomes

  • To study 3-year disease free survival as a function of baseline and post radiotherapy immune cell composition.(3 years from last day of treatment date and/or to date of recurrence/relapse.)

Investigators

Sponsor Class
Research institution and hospital
Responsible Party
Principal Investigator
Principal Investigator

Dr Supriya Chopra

Tata Memorial Centre

Study Sites (1)

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